CASPR2 Antibody Disease Overview

In Limbic-Predominant Encephalopathy, there are usually no other coexistent ___.

CASPR2 antibodies are linked to ___, a condition where the immune system mistakenly attacks the brain.

CASPR2 antibody disease primarily affects older males, typically in their ___ and ___.

___ shows encephalopathy in patients with CASPR2 antibody disease.

Morvan Syndrome symptoms include severe autonomic dysfunction, ___, peripheral nerve hyperexcitability, and psychiatric symptoms.

In diagnostic investigations for CASPR2 antibody disease, ___ and ___ are often normal.

The male-to-female ratio of CASPR2 antibody disease is about :.

Needle EMG detects peripheral nerve ___, which is a specific feature of CASPR2 antibody disease.

Immunotherapies are more effective in patients with ___ antibodies compared to those with CASPR2 antibodies.

The disease typically develops over several ___, which can overlap with more rapid neurodegenerative conditions like Creutzfeldt-Jakob disease.

Neuropathic pain in Morvan syndrome is possibly due to small fiber ___.

Higher titers in ___ help reduce false positives in antibody testing for CASPR2 antibody disease.

Limbic-Predominant Encephalopathy symptoms include ___, ___, and ___.

Approximately ___% of patients with Morvan Syndrome have a thymoma.

Movement disorders associated with CASPR2 antibody disease include ataxia, myoclonus, tremor, paroxysmal ataxia, and orthostatic leg ___.